TNSN97108A1 - Analogues d'indazole nouveaux - Google Patents

Analogues d'indazole nouveaux

Info

Publication number
TNSN97108A1
TNSN97108A1 TNTNSN97108A TNSN97108A TNSN97108A1 TN SN97108 A1 TNSN97108 A1 TN SN97108A1 TN TNSN97108 A TNTNSN97108 A TN TNSN97108A TN SN97108 A TNSN97108 A TN SN97108A TN SN97108 A1 TNSN97108 A1 TN SN97108A1
Authority
TN
Tunisia
Prior art keywords
preparation
indazole analogs
new indazole
new
analogs
Prior art date
Application number
TNTNSN97108A
Other languages
English (en)
Inventor
Marfat Anthony
Original Assignee
Pfizer
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pfizer filed Critical Pfizer
Publication of TNSN97108A1 publication Critical patent/TNSN97108A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/415—1,2-Diazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pain & Pain Management (AREA)
  • Obesity (AREA)
  • Neurosurgery (AREA)
  • Communicable Diseases (AREA)
  • Rheumatology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Immunology (AREA)
  • Urology & Nephrology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pulmonology (AREA)
  • Dermatology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

L' INVENTION CONCERNE DES COMPOSES DE FORMULE (1) : DANS LAQUELLE R, R1 ET R2 REPRESENTENT DIVERS RADICAUX. ELLE CONCERNE EGALEMENT DES PROCEDES POUR LEUR PREPARATION AINSI QUE DES COMPOSITIONS LES CONTENANT. APPLICATION : PREPARATION DE MEDICAMENTS DESTINES A INHIBER LA PHOSPHODIESTERASE (PDE) DE TYPE IV OU LA PRODUCTION DU FACTEUR DE NECROSE DE TUMEUR (TNF) CHEZ UN MAMMIFERE
TNTNSN97108A 1996-06-25 1997-06-24 Analogues d'indazole nouveaux TNSN97108A1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US2038596P 1996-06-25 1996-06-25

Publications (1)

Publication Number Publication Date
TNSN97108A1 true TNSN97108A1 (fr) 2005-03-15

Family

ID=21798354

Family Applications (1)

Application Number Title Priority Date Filing Date
TNTNSN97108A TNSN97108A1 (fr) 1996-06-25 1997-06-24 Analogues d'indazole nouveaux

Country Status (43)

Country Link
US (1) US6040329A (fr)
EP (1) EP0912558B1 (fr)
JP (1) JP3152940B2 (fr)
KR (1) KR20000022516A (fr)
CN (1) CN1080260C (fr)
AP (1) AP1025A (fr)
AR (1) AR007456A1 (fr)
AT (1) ATE244713T1 (fr)
AU (1) AU716376B2 (fr)
BG (1) BG64052B1 (fr)
BR (1) BR9712782A (fr)
CA (1) CA2258285C (fr)
CO (1) CO4900056A1 (fr)
CZ (1) CZ423398A3 (fr)
DE (1) DE69723447T2 (fr)
DK (1) DK0912558T3 (fr)
DZ (1) DZ2254A1 (fr)
EA (1) EA002274B1 (fr)
ES (1) ES2201299T3 (fr)
GT (1) GT199700075A (fr)
HK (1) HK1018700A1 (fr)
HN (1) HN1997000079A (fr)
HR (1) HRP970350B1 (fr)
HU (1) HUP9903009A3 (fr)
ID (1) ID18579A (fr)
IL (1) IL127036A (fr)
IS (1) IS4910A (fr)
MA (1) MA24225A1 (fr)
MY (1) MY116915A (fr)
NO (1) NO986103L (fr)
NZ (1) NZ332752A (fr)
OA (1) OA10934A (fr)
PA (1) PA8432301A1 (fr)
PL (1) PL330974A1 (fr)
PT (1) PT912558E (fr)
SI (1) SI0912558T1 (fr)
SK (1) SK176598A3 (fr)
TN (1) TNSN97108A1 (fr)
TR (1) TR199802685T2 (fr)
TW (1) TW434237B (fr)
WO (1) WO1997049702A1 (fr)
YU (1) YU60198A (fr)
ZA (1) ZA975581B (fr)

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BR9712005A (pt) * 1996-09-04 1999-08-24 Pfizer Derivados de indazol e seus usos como inibidores de fosfodiesterase (pde) tipo IV e produ-Æo do fator de necrose de tumor (tnf)
US6248746B1 (en) 1998-01-07 2001-06-19 Euro-Celtique S.A. 3-(arylalkyl) xanthines
ID24942A (id) * 1997-11-04 2000-08-31 Pfizer Prod Inc Senyawa terapi aktif yang berdasarkan penggantian bioisoster katekol dengan indazole pada inhibitor pde4
US6362213B1 (en) 1999-12-23 2002-03-26 Icos Corporation Cyclic AMP-specific phosphodiesterase inhibitors
EP1244649B1 (fr) * 1999-12-23 2005-03-02 Icos Corporation Inhibiteurs de phosphodiesterase specifique d'amp cyclique
US6953774B2 (en) 2000-08-11 2005-10-11 Applied Research Systems Ars Holding N.V. Methods of inducing ovulation
US7205320B2 (en) 2001-01-22 2007-04-17 Memory Pharmaceuticals Corp. Phosphodiesterase 4 inhibitors
US7153871B2 (en) 2001-01-22 2006-12-26 Memory Pharmaceuticals Corporation Phosphodiesterase 4 inhibitors, including aminoindazole and aminobenzofuran analogs
CN1300116C (zh) * 2001-04-16 2007-02-14 卫材株式会社 1h－吲唑化合物
BRPI0117198B1 (pt) 2001-12-14 2018-03-13 Merck Serono S.A. Usos de composição compreendendo um inibidor seletivo de uma isoforma 4 de fosfodiesterase
CN100381425C (zh) * 2002-07-19 2008-04-16 记忆药物公司 作为磷酸二酯酶4抑制剂的6-氨基-1h-吲唑及其药物组合物和用途
MXPA05000827A (es) 2002-07-19 2005-08-29 Memory Pharm Corp Inhibidores de fosfodiesterasa 4, incluyendo analogos de anilina y difenilamina n-sustituidos.
CN100513397C (zh) 2002-11-19 2009-07-15 记忆药物公司 磷酸二酯酶4抑制剂
RU2379292C2 (ru) * 2003-04-18 2010-01-20 Мемори Фармасьютиклз Корпорейшн Производные пиразола в качестве ингибиторов фосфодиэстеразы 4
US20090048255A1 (en) * 2003-07-21 2009-02-19 Schumacher Richard A Phosphodiesterase 4 inhibitors, including n-substituted aniline and diphenylamine analogs
MY141255A (en) * 2003-12-11 2010-03-31 Memory Pharm Corp Phosphodiesterase 4 inhibitors, including n-substituted diarylamine analogs
CN101166733A (zh) 2004-10-15 2008-04-23 记忆药物公司 作为磷酸二酯酶4抑制剂的吡唑衍生物
US7601847B2 (en) 2004-10-26 2009-10-13 Wyeth Preparation and purification of 4-(indazol-3-yl)phenols
WO2006129158A2 (fr) * 2005-05-30 2006-12-07 Ranbaxy Laboratories Limited Inhibiteurs de la phosphodiesterase de type iv
JP2009506069A (ja) 2005-08-26 2009-02-12 ブレインセルス，インコーポレイティド ムスカリン性受容体調節による神経発生
EP2258359A3 (fr) 2005-08-26 2011-04-06 Braincells, Inc. Neurogenèse par modulation des récepteurs muscariniques avec sabcomeline
US7781460B2 (en) 2005-09-05 2010-08-24 Ranbaxy Laboratories Limited Substituted indazoles as inhibitors of phosphodiesterase type-IV
US7915286B2 (en) 2005-09-16 2011-03-29 Ranbaxy Laboratories Limited Substituted pyrazolo [3,4-b] pyridines as phosphodiesterase inhibitors
AU2006304787A1 (en) 2005-10-21 2007-04-26 Braincells, Inc. Modulation of neurogenesis by PDE inhibition
CA2625210A1 (fr) 2005-10-31 2007-05-10 Braincells, Inc. Modulation de la neurogenese dont la mediation est assuree par recepteur gaba
US20100216734A1 (en) 2006-03-08 2010-08-26 Braincells, Inc. Modulation of neurogenesis by nootropic agents
AU2007249399A1 (en) 2006-05-09 2007-11-22 Braincells, Inc. Neurogenesis by modulating angiotensin
US20100184806A1 (en) 2006-09-19 2010-07-22 Braincells, Inc. Modulation of neurogenesis by ppar agents
MX2009009793A (es) 2007-03-14 2009-10-16 Ranbaxy Lab Ltd Derivados de pirazolo (3,4-b) piridina como inhibidores de fosfodiesterasa.
US20100029689A1 (en) * 2008-07-02 2010-02-04 Memory Pharmaceuticals Corporation Phosphodiesterase 4 inhibitors
WO2010099217A1 (fr) 2009-02-25 2010-09-02 Braincells, Inc. Modulation de neurogenèse à l'aide de combinaisons de d-cyclosérine
EP2493889B1 (fr) * 2009-10-30 2017-09-06 Janssen Pharmaceutica, N.V. Dérivés d'imidazo[1,2-b]pyridazine et leur utilisation en tant qu'inhibiteurs pde10
WO2013106547A1 (fr) 2012-01-10 2013-07-18 President And Fellows Of Harvard College Composés promoteurs de réplication des cellules bêta et leurs procédés d'utilisation
US20150125438A1 (en) * 2012-07-20 2015-05-07 Sang Jae Kim Anti-Inflammatory Peptides and Composition Comprising the Same
EP3137454A1 (fr) 2014-04-28 2017-03-08 Pfizer Inc. Composés hétéroaromatiques et leur utilisation en tant que ligands de la dopamine d1
KR20220167441A (ko) * 2021-06-11 2022-12-21 주식회사 메타센테라퓨틱스 신규한 인돌 유도체 및 이의 최종당화산물 관련 질환의 치료 용도
KR20220167804A (ko) * 2021-06-11 2022-12-22 주식회사 메타센테라퓨틱스 인돌 유도체를 포함하는 최종당화산물 관련 질환의 치료용 조성물

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Also Published As

Publication number Publication date
ES2201299T3 (es) 2004-03-16
DZ2254A1 (fr) 2002-12-18
EA199801047A1 (ru) 1999-06-24
SK176598A3 (en) 2000-06-12
BG103056A (en) 1999-10-29
DK0912558T3 (da) 2003-08-18
EA002274B1 (ru) 2002-02-28
HRP970350B1 (en) 2003-04-30
NZ332752A (en) 2001-04-27
HRP970350A2 (en) 1998-06-30
HN1997000079A (es) 1997-12-26
ID18579A (id) 1998-04-23
YU60198A (sh) 1999-09-27
NO986103D0 (no) 1998-12-23
JPH11514668A (ja) 1999-12-14
EP0912558A1 (fr) 1999-05-06
PT912558E (pt) 2003-11-28
JP3152940B2 (ja) 2001-04-03
IS4910A (is) 1998-11-27
TR199802685T2 (xx) 1999-03-22
ZA975581B (en) 1998-12-24
NO986103L (no) 1998-12-23
CN1080260C (zh) 2002-03-06
AU716376B2 (en) 2000-02-24
CA2258285A1 (fr) 1997-12-31
CA2258285C (fr) 2002-11-26
OA10934A (en) 2002-02-18
HK1018700A1 (en) 1999-12-30
MA24225A1 (fr) 1997-12-31
HUP9903009A2 (hu) 2000-05-28
PA8432301A1 (es) 1999-12-27
DE69723447D1 (de) 2003-08-14
EP0912558B1 (fr) 2003-07-09
WO1997049702A1 (fr) 1997-12-31
PL330974A1 (en) 1999-06-21
BR9712782A (pt) 1999-12-07
TW434237B (en) 2001-05-16
KR20000022516A (ko) 2000-04-25
DE69723447T2 (de) 2003-12-24
SI0912558T1 (en) 2003-10-31
IL127036A0 (en) 1999-09-22
ATE244713T1 (de) 2003-07-15
AP1025A (en) 2001-11-19
IL127036A (en) 2001-06-14
CO4900056A1 (es) 2000-03-27
HUP9903009A3 (en) 2002-01-28
CZ423398A3 (cs) 1999-12-15
CN1223651A (zh) 1999-07-21
GT199700075A (es) 1998-12-04
MY116915A (en) 2004-04-30
AR007456A1 (es) 1999-10-27
BG64052B1 (bg) 2003-11-28
AU2785797A (en) 1998-01-14
US6040329A (en) 2000-03-21
AP9701020A0 (en) 1997-07-31

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